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Rabson-Mendenhall syndrome
Sarita Kumar1, Milind S Tullu, Mamta N Muranjan
1The Genetics Division, Department of Pediatrics, Seth G. S. Medical College and KEM Hospital, Parel, Mumbai 400 012, India.
Abstract:
Rabson-Mendenhall syndrome is characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, premature and dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia and post-prandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. We describe a six-month-old female child with physical features suggestive of the Rabson-Mendenhall syndrome. The child also had medullary nephrocalcinosis.
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